510(k) K925250 ยท HHD Pad, Menstrual, Unscented
KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS
| Applicant | Kimberly-Clark Corp., Washington DC, US |
| Decision | Substantially Equivalent, Mar 3, 1993 |
| Received | Oct 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925250
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.